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柴胡皂苷 A 通过 ROS 积累诱导细胞凋亡和通过 NF-κB 通路抑制炎症来靶向 HEKa 细胞的细胞毒性。

Cytotoxicity of Saikosaponin A targets HEKa cell through apoptosis induction by ROS accumulation and inflammation suppression via NF-κB pathway.

机构信息

Dermatology, Xi'an Jiaotong University Second Affiliated Hospital, Xi'an, Shaanxi 710004, China.

Center for Mitochondrial Biology and Medicine, The Key Laboratory of Biomedical Information Engineering of Minstry of Education, Xi'an Jiaotong University School of Life Science and Technology, Xi'an, Shaanxi 710049, China.

出版信息

Int Immunopharmacol. 2020 Sep;86:106751. doi: 10.1016/j.intimp.2020.106751. Epub 2020 Jul 4.

Abstract

Saikosaponin A (SSA) is a triterpenoid saponin extracted from oriental medicinal plant Radix bupleuri, possessing various biological functions such as anti-inflammatory, immune regulation and anti-virus. This study aimed to explore therapeutic effects of SSA on psoriasis in both vitro and vivo. Our results showed that SSA increased reactive oxygen species (ROS) generation, and decreased mitochondrial membrane potential (MMP) and M5-induced inflammatory cytokines levels in HEKa cells in a dose-dependent manner. In addition, SSA promoted apoptosis and suppressed phosphorylation of NF-κB in vitro, which were restored by the ROS scavenger N-acetylcysteine (NAC). In imiquimod (IMQ)-induced mice, gavage with SSA markedly decreased Psoriasis Area and Severity Index (PASI) score and ameliorated epidermal hyperplasia through inhibition of NF-κB and NLRP3 signaling pathway. In conclusion, our studies demonstrate that SSA induces apoptosis and suppresses inflammation in HEKa cells and ameliorates IMQ-induced psoriasis in mice, making it a therapeutic candidate for psoriasis.

摘要

柴胡皂苷 A(SSA)是从东方药用植物柴胡中提取的一种三萜皂苷,具有抗炎、免疫调节和抗病毒等多种生物学功能。本研究旨在探讨 SSA 在体内外对银屑病的治疗作用。我们的研究结果表明,SSA 可剂量依赖性地增加 HEKa 细胞中活性氧(ROS)的产生,降低线粒体膜电位(MMP)和 M5 诱导的炎症细胞因子水平。此外,SSA 可促进体外细胞凋亡并抑制 NF-κB 的磷酸化,而 ROS 清除剂 N-乙酰半胱氨酸(NAC)可恢复这一作用。在咪喹莫特(IMQ)诱导的小鼠中,SSA 通过抑制 NF-κB 和 NLRP3 信号通路,显著降低银屑病面积和严重程度指数(PASI)评分并改善表皮增生。综上所述,我们的研究表明 SSA 可诱导 HEKa 细胞凋亡并抑制炎症,改善 IMQ 诱导的小鼠银屑病,使其成为银屑病的治疗候选药物。

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